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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259931Generated: November 1, 2026

Benzyl Bromide → Ethyl-N-Benzenesulfonyl-4-(benzyl)-piperidine-4-carboxylate

https://huagongshe.com/reaction/2259931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantEthyl 1-(phenylsulfonyl)piperidine-4-carboxylateHCID 257103—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
ProductEthyl-N-Benzenesulfonyl-4-(benzyl)-piperidine-4-carboxylateHCID 19962183—

Reaction Steps

A solution of ethyl-N-benzenesulfonyl-isonipecotate (5 g, 0.016 mole) in tetrahydrofuran (1 L) at -78° C. was treated with a solution of Lithium bis (trimethylsilyl)amide in tetrahydrofuran (18.5 mL of a 1M solution). The solution was stirred at -60° for 15 minutes at which time benzyl bromide (3.15 g, 0.016 moles) was added and the reaction warmed to room temperature over 1.5 hours. The reaction was concentrated at reduced pressure to @ one quarter volume and then poured into saturated aqueous sodium bicarbonate (1 L) and extracted with ethyl acetate (2×800 mL). The combined extracts were dried over anhydrous magnesium sulfate, filtered, and concentrated at reduced pressure. The residue was chromatographed on silica gel with 30% ethyl acetate/hexane as eluent to give 5.1 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05475109
Source datasetuspto-grants-1995_12
ORD IDord-26f444ddaf5f4e97b651e615b89c4689
Source noteuspto-grants-1995_12